Literature DB >> 22731514

Utilization of supportive and palliative care services among oncology outpatients at one academic cancer center: determinants of use and barriers to access.

Pallavi Kumar1, David Casarett, Amy Corcoran, Krupali Desai, Qing Li, Jinbo Chen, Corey Langer, Jun J Mao.   

Abstract

UNLABELLED: Abstract Background: Cancer causes significant symptom burden and diminished quality of life. Despite the expansion of supportive and palliative care services (SPCS), little is known about rates of utilization and barriers to access to these services among oncology outpatients.
METHODS: We performed a cross-sectional survey in three outpatient medical oncology clinics. Patients with a diagnosis of breast, lung, or gastrointestinal (GI) cancer and a Karnofsky score of ≥60 were included. Patients reported their use of SPCS and any perceived barriers. Multivariable logistic regression was used to identify factors associated with SPCS use.
RESULTS: Among 313 participants, (50.5%) had not used SPCS since cancer diagnosis. The most common services used were nutrition (26.5%), psychiatric/psychological counseling (29.7%), and physical therapy (15.1%). Pain/palliative care and cancer rehabilitation consultations were used by 8.5% and 4.1% of participants, respectively. In multivariate analysis, graduate education was associated with greater SPCS use (adjusted odds ratio [AOR] 2.14, 95% confidence interval [CI] 1.08-4.26) compared with those with high school or less, whereas having lung cancer was associated with less SPCS use (AOR 0.48, 95% CI 0.24-0.96) when compared with those having breast cancer. The biggest reported barriers to using SPCS were a lack of awareness (22.4%) and lack of physician referral (23%).
CONCLUSIONS: Approximately half of these patients had not accessed SPCS since cancer diagnosis and cite lack of awareness and physician nonreferral as barriers. Further research is needed to understand patients' needs and beliefs regarding SPCS, and how to integrate SPCS into conventional treatments to improve cancer care.

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Year:  2012        PMID: 22731514      PMCID: PMC3396135          DOI: 10.1089/jpm.2011.0217

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  59 in total

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Review 3.  Socioeconomic disparities in health: pathways and policies.

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5.  Cancer and comorbidity: redefining chronic diseases.

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Review 7.  Quality of life concerns in patients with breast cancer: evidence for disparity of outcomes and experiences in pain management and palliative care among African-American women.

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Review 9.  Cancer disparities by race/ethnicity and socioeconomic status.

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  33 in total

1.  Supportive care needs and preferences of lung cancer patients: a semi-structured qualitative interview study.

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Journal:  Support Care Cancer       Date:  2014-11-14       Impact factor: 3.603

2.  Integrating Oncology Massage Into Chemoinfusion Suites: A Program Evaluation.

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3.  Statewide Differences in Personality Associated with Geographic Disparities in Access to Palliative Care: Findings on Openness.

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4.  Impact of Interdisciplinary Outpatient Specialty Palliative Care on Survival and Quality of Life in Adults With Advanced Cancer: A Meta-Analysis of Randomized Controlled Trials.

Authors:  Michael Hoerger; Graceanne R Wayser; Gregory Schwing; Ayako Suzuki; Laura M Perry
Journal:  Ann Behav Med       Date:  2019-06-04

5.  Toward a Broader Role for Occupational Therapy in Supportive Oncology Care.

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6.  Does educating patients about the Early Palliative Care Study increase preferences for outpatient palliative cancer care? Findings from Project EMPOWER.

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Journal:  Health Psychol       Date:  2017-03-09       Impact factor: 4.267

7.  ReCAP: Attitudes, Beliefs, and Awareness of Graduate Medical Education Trainees Regarding Palliative Care at a Comprehensive Cancer Center.

Authors:  Angelique Wong; Akhila Reddy; Janet L Williams; Jimin Wu; Diane Liu; Eduardo Bruera; Angelique Wong; Akhila Reddy; Janet L Williams; Jimin Wu; Diane Liu; Eduardo Bruera
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8.  Use of inpatient palliative care services in patients with metastatic incurable head and neck cancer.

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Journal:  Am J Hosp Palliat Care       Date:  2013-04-23       Impact factor: 2.500

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